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ERX2006539: Illumina Genome Analyzer II paired end sequencing
1 ILLUMINA (Illumina Genome Analyzer II) run: 303 spots, 48,480 bases, 65,053b downloads

Design: Illumina sequencing of library NT220442K, constructed from sample accession ERS016359 for study accession ERP000111. This is part of an Illumina multiplexed sequencing run (5505_8). This submission includes reads tagged with the sequence GCCAATGTAT.
Submitted by: SC (The Wellcome Trust Sanger Institute)
Study: Epidemiology of tuberculosis
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For further information on this study please see http://www.sanger.ac.uk/resources/downloads/bacteria/mycobacterium.html
Sample:
SAMEA968126 • ERS016359 • All experiments • All runs
Library:
Name: NT220442K
Instrument: Illumina Genome Analyzer II
Strategy: WGS
Source: GENOMIC
Selection: RANDOM
Layout: PAIRED
Construction protocol: Standard
Runs: 1 run, 303 spots, 48,480 bases, 65,053b
Run# of Spots# of BasesSizePublished
ERR02920830348,48065,053b2011-03-18

ID:
3966166

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